Fingerprint
Dive into the research topics of '17β-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17βHSD3 gene'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
17β-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17βHSD3 gene
Ayfer Alikasifoglu*, Olaf Hiort, Nazli Gonc, Huseyin Demirbilek, Emregul Isik, Nurgun Kandemir
*Corresponding author for this work
17
Citations
(Scopus)